packages
[ 源代码: snippy ]
软件包: snippy (4.6.0+dfsg-5) [universe]
snippy 的相关链接
Ubuntu 的资源:
下载源码包 snippy:
维护者:
Please consider filing a bug or asking a question via Launchpad before contacting the maintainer directly.
Original Maintainers (usually from Debian):
- Debian Med Packaging Team (Mail Archive)
- Andreas Tille
It should generally not be necessary for users to contact the original maintainer.
外部的资源:
- 主页 [github.com]
相似软件包:
rapid haploid variant calling and core genome alignment
其他与 snippy 有关的软件包
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- dep: any2fasta
- convert various sequence formats to FASTA
-
- dep: bcftools
- genomic variant calling and manipulation of VCF/BCF files
-
- dep: bedtools
- suite of utilities for comparing genomic features
-
- dep: bwa
- Burrows-Wheeler Aligner
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- dep: freebayes (>= 1.3.6-2)
- Bayesian haplotype-based polymorphism discovery and genotyping
-
- dep: libbio-perl-perl
- BioPerl core perl modules
-
- dep: libvcflib-tools
- C++ library for parsing and manipulating VCF files (tools)
-
- dep: minimap2
- versatile pairwise aligner for genomic and spliced nucleotide sequences
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- dep: parallel
- build and execute command lines from standard input in parallel
-
- dep: perl
- Larry Wall's Practical Extraction and Report Language
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- dep: samclip
- filter SAM file for soft and hard clipped alignments
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- dep: samtools
- processing sequence alignments in SAM, BAM and CRAM formats
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- dep: seqtk
- Fast and lightweight tool for processing sequences in the FASTA or FASTQ format
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- dep: snp-sites
- Binary code for the package snp-sites
-
- dep: snpeff
- genetic variant annotation and effect prediction toolbox - tool
-
- dep: vt
- toolset for short variant discovery in genetic sequence data